EP0676751A1 - Optisches Aufzeichnungsmedium - Google Patents
Optisches Aufzeichnungsmedium Download PDFInfo
- Publication number
- EP0676751A1 EP0676751A1 EP95105296A EP95105296A EP0676751A1 EP 0676751 A1 EP0676751 A1 EP 0676751A1 EP 95105296 A EP95105296 A EP 95105296A EP 95105296 A EP95105296 A EP 95105296A EP 0676751 A1 EP0676751 A1 EP 0676751A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- wavelength
- dye
- layer
- recording
- light beam
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 230000003287 optical effect Effects 0.000 title claims abstract description 109
- 239000000975 dye Substances 0.000 claims abstract description 225
- 239000000758 substrate Substances 0.000 claims abstract description 68
- 238000010521 absorption reaction Methods 0.000 claims abstract description 54
- 239000000987 azo dye Substances 0.000 claims abstract description 29
- 239000001007 phthalocyanine dye Substances 0.000 claims abstract description 27
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 47
- 238000002835 absorbance Methods 0.000 claims description 27
- 229910052751 metal Inorganic materials 0.000 claims description 19
- 239000002184 metal Substances 0.000 claims description 19
- 239000010931 gold Substances 0.000 claims description 13
- 150000004696 coordination complex Chemical class 0.000 claims description 11
- 150000002739 metals Chemical class 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 229910052737 gold Inorganic materials 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 6
- 150000004032 porphyrins Chemical class 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- YKENVNAJIQUGKU-UHFFFAOYSA-N tetraazaporphin Chemical compound C=1C(C=N2)=NC2=NC(NN2)=NC2=CC(C=C2)=NC2=CC2=NC=1C=C2 YKENVNAJIQUGKU-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 229910001507 metal halide Inorganic materials 0.000 claims description 3
- 150000005309 metal halides Chemical class 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 1
- 239000010410 layer Substances 0.000 description 236
- 125000001424 substituent group Chemical group 0.000 description 82
- 239000010408 film Substances 0.000 description 66
- 239000004065 semiconductor Substances 0.000 description 42
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 40
- 238000004528 spin coating Methods 0.000 description 33
- 230000000052 comparative effect Effects 0.000 description 27
- 229920005989 resin Polymers 0.000 description 27
- 239000011347 resin Substances 0.000 description 27
- 238000004544 sputter deposition Methods 0.000 description 27
- -1 dimethylcyclohexyl group Chemical group 0.000 description 24
- 230000035945 sensitivity Effects 0.000 description 16
- NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 13
- 230000003595 spectral effect Effects 0.000 description 13
- GDIYMWAMJKRXRE-UHFFFAOYSA-N (2z)-2-[(2e)-2-[2-chloro-3-[(z)-2-(1,3,3-trimethylindol-1-ium-2-yl)ethenyl]cyclohex-2-en-1-ylidene]ethylidene]-1,3,3-trimethylindole Chemical compound CC1(C)C2=CC=CC=C2N(C)C1=CC=C1C(Cl)=C(C=CC=2C(C3=CC=CC=C3[N+]=2C)(C)C)CCC1 GDIYMWAMJKRXRE-UHFFFAOYSA-N 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 239000011241 protective layer Substances 0.000 description 12
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 10
- 125000003545 alkoxy group Chemical group 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000000151 deposition Methods 0.000 description 7
- 229920000515 polycarbonate Polymers 0.000 description 7
- 239000004417 polycarbonate Substances 0.000 description 7
- 239000010409 thin film Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 125000004414 alkyl thio group Chemical group 0.000 description 6
- 125000004093 cyano group Chemical group *C#N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 150000004820 halides Chemical group 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 5
- 229910010272 inorganic material Inorganic materials 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- 239000012454 non-polar solvent Substances 0.000 description 5
- 239000002798 polar solvent Substances 0.000 description 5
- KVZJLSYJROEPSQ-UHFFFAOYSA-N 1,2-dimethylcyclohexane Chemical compound CC1CCCCC1C KVZJLSYJROEPSQ-UHFFFAOYSA-N 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000004442 acylamino group Chemical group 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 230000031700 light absorption Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 125000000565 sulfonamide group Chemical group 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- 229910006069 SO3H Inorganic materials 0.000 description 3
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 150000002484 inorganic compounds Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 238000001771 vacuum deposition Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 2
- MEBONNVPKOBPEA-UHFFFAOYSA-N 1,1,2-trimethylcyclohexane Chemical compound CC1CCCCC1(C)C MEBONNVPKOBPEA-UHFFFAOYSA-N 0.000 description 2
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- VZBILKJHDPEENF-UHFFFAOYSA-M C3-thiacarbocyanine Chemical compound [I-].S1C2=CC=CC=C2[N+](CC)=C1C=CC=C1N(CC)C2=CC=CC=C2S1 VZBILKJHDPEENF-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229930192627 Naphthoquinone Natural products 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000002521 alkyl halide group Chemical group 0.000 description 2
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 2
- 239000001000 anthraquinone dye Substances 0.000 description 2
- 125000005110 aryl thio group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 125000003709 fluoroalkyl group Chemical group 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 150000002791 naphthoquinones Chemical class 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 2
- DEDZSLCZHWTGOR-UHFFFAOYSA-N propylcyclohexane Chemical compound CCCC1CCCCC1 DEDZSLCZHWTGOR-UHFFFAOYSA-N 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000002411 thermogravimetry Methods 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- CSUFEOXMCRPQBB-UHFFFAOYSA-N 1,1,2,2-tetrafluoropropan-1-ol Chemical compound CC(F)(F)C(O)(F)F CSUFEOXMCRPQBB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- JUGSKHLZINSXPQ-UHFFFAOYSA-N 2,2,3,3,4,4,5,5-octafluoropentan-1-ol Chemical compound OCC(F)(F)C(F)(F)C(F)(F)C(F)F JUGSKHLZINSXPQ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- ORIHZIZPTZTNCU-VMPITWQZSA-N 2-[(E)-hydroxyiminomethyl]phenol Chemical compound O\N=C\C1=CC=CC=C1O ORIHZIZPTZTNCU-VMPITWQZSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910006074 SO2NH2 Inorganic materials 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- BBAWTPDTGRXPDG-UHFFFAOYSA-N [1,3]thiazolo[4,5-b]pyridine Chemical group C1=CC=C2SC=NC2=N1 BBAWTPDTGRXPDG-UHFFFAOYSA-N 0.000 description 1
- OTNSELQCFOLCCA-UHFFFAOYSA-N [1,3]thiazolo[4,5-b]quinoline Chemical group C1=CC=C2C=C(SC=N3)C3=NC2=C1 OTNSELQCFOLCCA-UHFFFAOYSA-N 0.000 description 1
- RIUVLOXDBAJYGF-UHFFFAOYSA-N [1,3]thiazolo[5,4-f]quinoline Chemical group N1=CC=CC2=C(SC=N3)C3=CC=C21 RIUVLOXDBAJYGF-UHFFFAOYSA-N 0.000 description 1
- 239000000999 acridine dye Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005055 alkyl alkoxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 125000005157 alkyl carboxy group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical class Br* 0.000 description 1
- HLKZFSVWBQSKKH-UHFFFAOYSA-N but-3-enoic acid;1-ethenylpyrrolidin-2-one Chemical compound OC(=O)CC=C.C=CN1CCCC1=O HLKZFSVWBQSKKH-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
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- 238000005229 chemical vapour deposition Methods 0.000 description 1
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Classifications
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-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/146—Laser beam
Definitions
- the present invention relates to an optical recording medium having at least a dye-containing recording layer and a reflective layer formed on a transparent substrate. More particularly, the present invention relates to an optical recording medium which satisfies the Orange Book Standards for compact disc-recordable (hereinafter, referred to as CD-R), allowing recording and reproduction of information by using a laser beam having a selected wavelength of from 770 to 830 nm as well as allowing reproduction by using a laser beam having a selected wavelength of from 630 to 690 nm.
- CD-R Orange Book Standards for compact disc-recordable
- CD-Rs Conventional single-substrate recordable optical disc, CD-Rs, are disclosed in, for example, "Optical Data Storage 1989", Technical Digest Series, Vol. 1, 45 (1989), in which the medium has a recording layer of dyes, a metal reflective layer provided on the recording layer to improve the reflectance, and a protective layer provided on the latter.
- the recording layer of the media may contain cyanine dyes or phthalocyanine dyes of the type used in the present invention.
- Such recording media are available on the market as a compact disc-recordable (CD-R).
- the CD-R medium is based on the Orange Book Standards and has a reflectance of 65% or higher to a beam having a selected wavelength ( ⁇ 1) of from 770 to 830 nm while absorbing the beam having the wavelength ⁇ 1.
- Information can thus be recorded on such a medium by using a semiconductor laser of 780 nm.
- the recorded information can be reproduced through a commercially available CD player or CD-ROM player provided with a semiconductor laser of 780 nm.
- optical recording media currently available have a recording capacity of only 650 MB.
- a recording time is thus 15 minutes at maximum for recording a large volume of information such as dynamic digital images.
- conventional recording density cannot provide a sufficient memory capacity as the medium becomes small.
- a semiconductor laser having a wavelength ( ⁇ 2) selected from 630 to 690 nm has been developed.
- This semiconductor laser is making it possible to achieve high-density recording and/or reproduction. It has been studied to develop, with this semiconductor laser, a high-density recording medium having 5-8 times the recording capacity of conventional media and to develop a CD player for such high-density recording media which is capable of reproducing information thereon. In particular, there have been studied systems capable of recording a movie of 2 hours or more in digital format. Read-only media and reproduction players for such systems are to be introduced into the market as digital video discs (DVDs).
- DVDs digital video discs
- this high-density recording media there is a read-only medium having an aluminum reflective layer deposited on the pits formed in producing the substrate, as in the conventional CD and CD-ROM media.
- This read-only high-density recording medium has a reflectance of 70% or higher. It is thus necessary that a player capable of reproducing such high-density recording media is designed to have a capability of reproducing information on the read-only medium having the reflectance of 70% or higher.
- this high-density player is desired to be able to read conventional media such as CDs, CD-ROMs, and CD-Rs.
- CD and CD-ROM media are for read-only purpose, and the process of manufacturing them is the same as that for the above mentioned high-density read-only media. These media have a reflectance of 70% or higher and are thus applicable to the high-density player for reproduction.
- the conventional CD-R media currently available in the market have a reflectance of 65% or higher to the light beam having a wavelength of about 780 nm and are applicable to a commercially available CD or CD-ROM player.
- these media have a reflectance of 10% or smaller when subjected to reproduction with a light beam having a wavelength ( ⁇ 2) selected from the range of 630-690 nm.
- the degree of modulation is small and the reflectance of a recorded portion becomes larger than that of an unrecorded portion.
- This phenomenon is known as "low to high recording", in which the polarity is reversed from common CDs (high to low recording).
- a resultant reproduced signals have a large deformation. Due to these various disadvantages, it is difficult to play the conventional CD-R media by using a player for high-density media with a laser beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm.
- U.S. Patent No. 5,090,009 discloses a CD-R medium comprising a dye-containing recording layer, a reflective layer, and a protective layer laminated on a substrate in this order.
- This patent also discloses a medium having an interference layer provided between the substrate and the recording layer or between the recording layer and the reflective layer.
- optical constants as well as a film thickness of the recording layer to satisfy the CD standards (Red Book) and to enable recording.
- the media disclosed certainly absorb a portion of the light beam of 780 nm which is used for CDs.
- the reflectance of the media can be 70% or higher. The CDs are thus recordable and reproducible with the light beam of this wavelength.
- the '009 patent is, however, not directed to recording and reproduction with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm.
- the '009 patent discloses various examples of the media having a recording layer of an indodicarbocyanine dye, of which some media have an interference layer made of an inorganic compound or a polymer, and others not.
- the media with the recording layer of the indodicarbocyanine dye have the reflectance of 10% or lower to the light beam having the wavelength selected from the range between 630 and 690 nm.
- the recording is the low to high recording, in which the reflectance of the recorded portion is larger than that of the unrecorded portion.
- the reasons of this small reflectance are as follows: the optical characteristics of the dye used is highly dependent on the wavelengths.
- the above mentioned indodicarbocyanine dye has a significantly large absorption at from 600 to 750 nm when measured on the recording layer; and the CD-R medium has the optical constants (refractive index which is the value of the real part of the complex refractive index, and attenuation coefficient which is the absolute value of the imaginary part of the complex refractive index) and the film thickness designed to achieve a high reflectance to the light beam of around 780 nm.
- the reflectance is small at the wavelengths within the range between 630 and 690 nm.
- the Examples 8 and 14 of this patent disclose media having a recording layer of t -butyl substituted phthalocyanine dye, which is different from phthalocyanine dye used as the recording layer of the present invention, and an interference layer made of a polymer or an inorganic compound. Though the reflectance and the degree of modulation of these media satisfy the CD standards, a reproduced waveform has a large deformation when the signal recorded by pulse width modulation as in CDs is reproduced with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm. The error rate and the jitter value become large, and the media thus cannot be played back by a player for the high-density.
- European Patent Laid-Open No. 0 019 329 discloses a medium having a recording layer of VO-phthalocyanine dye, on which an interference layer of cellulose (300 nm) is applied.
- the application is, however, directed to improve the reflectance and the recording sensitivity to a specific single wavelength.
- the recording layer is not optimized to permit recording and reproduction with two light beams having the wavelength ( ⁇ 1) selected from the range between 770 and 830 nm and the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm, respectively.
- a reproduced waveform has a large deformation when the signal recorded by pulse width modulation as in CDs is reproduced with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm.
- the error rate and the jitter value become large, and the media thus cannot be played back by a player for the high-density.
- U.S. Patent No. 5,124,067 discloses dyes similar to those used in the recording layer of the present invention.
- the patent also discloses several media using such dyes.
- the media disclosed in Examples 98, 100, and 102 of the patent provide a recording mode of low-to-high when reproduced with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm.
- the reflectance is 10% or lower.
- a reproduced waveform has a large deformation when the signal recorded by pulse width modulation as in CDs is reproduced with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm. The error rate and the jitter value become large, and the media thus cannot be played back by a player for the high-density.
- Japanese Patent Laid-open No. 3-281287 discloses a medium having a recording layer of a mixture of dyes (A) and (B), in which the dye (A) has an absorption maximum of the longer wavelength at 780 nm and has such a complex refractive index that the absolute value of the imaginary part of the refractive index at 780 nm is 0.2 or smaller; and the dye (B) is a trimethine cyanine dye having an absorption maximum at a wavelength shorter than the wavelength at which the dye (A) exhibits the absorption maximum.
- This medium is superior in durability and satisfies the CD standards. However, it is not optimized for reproduction with the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm.
- the rate of the trimethine cyanine dye used is 50 wt.% and the rate of the pentamethine cyanine dye used is also 50 wt.%.
- the resultant medium thus has an excessively large absorption to the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm. As a result, the reflectance becomes lower than 15%, and it is thus difficult to reproduce the recorded information by using a player for the high-density.
- Japanese Patent Laid-open No. 6-336086 discloses a medium having a recording layer of a mixture of a trimethine cyanine dye and a pentamethine cyanine dye both of which have a specific structure. This medium is directed to recording and reproduction with the light beams having the wavelength of 780 nm and 488 nm. A ratio of the trimethine cyanine dye and the pentamethine cyanine dye is 1:10. With the larger rate of the pentamethine cyanine dye used, the resultant recording layer has an excessively larger absorption to the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm. As a result, the reflectance becomes lower than 15%, and it is thus difficult to reproduce the recorded information by using a player for the high-density.
- Japanese Patent Laid-open No. 6-40162 discloses a medium having a recording layer of a trimethine cyanine dye. This medium is directed to recording and reproduction with the light beam having the wavelength of 630 nm. The recording layer has no absorption to the light beam having the wavelength of 780 nm, so that the recording cannot be achieved with the light of this wavelength.
- Japanese Patent Laid-open No. 3-290835 discloses a medium provided with an interference layer made of a low molecular weight organic compound between a recording layer and a reflective layer of an aluminum alloy.
- This medium uses the aluminum alloy rather than expensive gold for the reflective layer, and has an interference layer to achieve the reflectance of 70% or higher at 780 nm.
- the reflectance is certainly 70% or higher at 780 nm.
- the reflectance is low to the light beam having the wavelength ( ⁇ 2) selected from the range between 630 and 690 nm, and it is thus difficult to reproduce the recorded information by using a player for the high-density.
- an optical recording medium having at least a dye-containing recording layer and a reflective layer as has a reflectance of 65% or higher to the laser beam having the wavelength ( ⁇ 1) selected from the range between 770 and 830 nm, has high sensitivity, is superior in recording characteristics, can be played back by a commercially available CD or CD-ROM player, and as can be played back also by a player for high-density with a laser beam having the selected wavelength ( ⁇ 2) of from 630 to 690 nm.
- the present inventors have made tremendous studies to develop a medium that satisfies the Orange Book Standards for CD-Rs (having a reflectance of 65% or higher to the light beam having the selected wavelength of from 770 to 830 nm and allowing recording and reproduction at that wavelength), and that can be recorded in a high-to-low recording mode without causing a deformation in a reproduced waveform when played back with the light beam having the selected wavelength of from 630 to 690 nm, and that the error rate and the jitter value are small.
- the present invention was thus completed.
- an optical recording medium having at least a dye-containing recording layer and a reflective layer laminated on a transparent substrate in this order, the medium having a reflectance of 65% or higher, measured through the substrate, to the light beam having a selected wavelength ( ⁇ 1) of from 770 to 830 nm and having a reflectance of 15% or higher, measured through the substrate, to the light beam having a selected wavelength ( ⁇ 2) of from 630 to 690 nm, the medium thereby being recordable and reproducible with a laser beam having the wavelength of ⁇ 1 and being reproducible with a laser beam having the wavelength of ⁇ 2.
- the optical recording medium according to the present invention has a reflectance of 65% or higher, measured through the substrate, to the light beam having a selected wavelength ( ⁇ 1) of from 770 to 830 nm and has a reflectance of 15% or higher, measured through the substrate, to the light beam having a selected wavelength ( ⁇ 2) of from 630 to 690 nm.
- Typical CD and CD-ROM players commercially available are provided with a semiconductor laser having a wavelength around 780 nm. In addition, such players are so designed as to be applicable to media having a reflectance of 65% or higher.
- the recording medium of the present invention can thus be played back with a commercially available CD or CD-ROM player.
- the reflectance of a medium reproducible with a player for high-density which is provided with a laser having a selected wavelength ( ⁇ 2) from 630 to 690 nm.
- ⁇ 2 a selected wavelength
- the players for high-density are designed to reproduce information from a read-only medium having a high reflectance of 70% or higher.
- the reflectance to the light beam having a selected wavelength ( ⁇ 2) of from 630 to 690 nm is 15% or higher, and more preferably 20% of higher.
- the medium according to the present invention may be either one of the following two alternative types:
- the transparent substrate used in the medium of type (a) according to the present invention preferably has a transmittance of 85% or higher to the light used for recording and reading signals, and has a small optical anisotropy.
- the transparent substrate may be, for example, made of a known resin such as an acrylic resin, a polycarbonate resin, and a polyolefin resin.
- the substrate may be in the form of a plate or of a film, and may be disc-shaped or card-shaped.
- On the surface of the substrate may be a spiral track of successive shallow depressions (pre-groove) or pits to store the digital information in the length thereof.
- pre-groove or pits are preferably formed in producing the substrate, they may be formed in an ultraviolet-curing resin layer formed on the substrate.
- optical characteristics of the dye-containing recording layer in the above mentioned medium (a) are important factors in respect to reflectance, recording sensitivity, and a degree of modulation. It is preferable that the following relationships hold: n1 ⁇ 1.8, 0.04 ⁇ k1 ⁇ 0.15, n2 ⁇ 1.6, and 0.04 ⁇ k2 ⁇ 0.4, where n1 is a value of the real part of the complex refractive index of the recording layer to a light beam having a wavelength of ⁇ 1, k1 is an absolute value of the imaginary part of the complex refractive index of the recording layer to a light beam of ⁇ 1, n2 is a value of the real part of the complex refractive index of the recording layer to a light beam having a wavelength of ⁇ 2, and k2 is an absolute value of the imaginary part of the complex refractive index of the recording layer to a light beam of ⁇ 2.
- the absorbance of the recording layer is preferably from 0.03 to 0.3 to the light beam of ⁇ 1, and from 0.03 to 0.5 to the light beam of ⁇ 2.
- n1 is smaller than 1.8 or when k1 is larger than 0.15, it becomes difficult to achieve the reflectance of 65% or higher to the light beam of ⁇ 1.
- k1 is smaller than 0.04, the recording sensitivity to the light beam of ⁇ 1 is deteriorated.
- n2 smaller than 1.6 and k2 larger than 0.4 are not preferable in that they cause the reflectance to the light beam of ⁇ 2 to be lower than 15%.
- k2 is 0.04 or larger in respect to the recording sensitivity to the light beam of ⁇ 2 because it is desirable that the light beam of ⁇ 2 can be used for recording.
- the recording layer has the absorbance smaller than 0.03 to the light beam of ⁇ 1, the recording sensitivity to the light beam of ⁇ 1 is deteriorated.
- the absorbance thereof exceeds 0.3, the reflectance to the light beam of ⁇ 1 becomes lower than 65%.
- the absorbance larger than 0.5 to the light beam of ⁇ 2 is not preferable in that it causes the reflectance to the light beam of ⁇ 2 to be smaller than 15%.
- the absorbance is 0.03 or larger in respect to the recording sensitivity to the light beam of ⁇ 2 because it is desirable that the light beam of ⁇ 2 can be used for recording.
- the present invention uses a dye A having the absorption maximum at the wavelength shorter than 630 nm mixed with a dye B having the absorption maximum at the wavelength of from 630 to 900 nm to impart the above mentioned optical characteristics to the recording layer. It is preferable that the rate of the dye A is in a range from 80 wt.% to 99.9 wt.%, both inclusive, and the rate of the dye B is in a range from 0.1 wt.% to 20 wt.%, both inclusive.
- the dyes A and B may be formed of two or more dyes.
- the dyes include phthalocyanine dyes, naphthalocyanine dyes, cyanine dyes, styryl dyes, merocyanine dyes, squarylium dyes, pyrylium dyes, anthraquinone dyes, naphthoquinone dyes, benzoquinone dyes, porphyrin dyes, azo dyes, dithiol metal complex dyes, indophenol dyes, triphenylmethane dyes, xanthene dyes, indanthrene dyes, indigo dyes, oxazine dyes, thiazine dyes, acridine dyes, indoaniline dyes, and azulenium dyes. These dyes may contain a metal or metals.
- heptamethine cyanine, phthalocyanine, and naphthalocyanine dyes are preferable as the dye B having the absorption maximum at between 630 and 900 nm in that they have a large molar absorption coefficient of the absorption maximum.
- Phthalocyanine and naphthalocyanine dyes are particularly preferable in that they exhibit remarkable resistance to light and moist heat.
- monocarbocyanine (trimethine cyanine), porphyrin, tetraazaporphyrin, and azo dyes are preferable in that they have a large molar absorption coefficient of the absorption maximum.
- monocarbocyanine is particularly preferable in that it has a larger molar absorption coefficient of the absorption maximum.
- the dye having the absorption maximum at between 630 and 900 nm is compatible with the dye having the absorption maximum at the wavelength shorter than 630 nm because they can be coated with being dissolved in a solvent.
- the term "absorption maximum” used herein means the absorption maximum or the absorption close to the maximum one at the individual ranges. If there are two or more peaks, this term means the one having the largest wavelength.
- light absorption characteristics of the dyes depend on a state of association of molecules. The light absorption characteristics are also different between in a solution phase and a solid phase (film), and depend on concentrations.
- the absorption maximum wavelength in the present invention is the value obtained when measured on a film containing a single kind of dye.
- the monocarbocyanine (trimethine cyanine) dyes include those obtained by means of adding a substituent or substituents to increase solubility to indocarbocyanine dyes, thiacarbocyanine dyes, quinooxacarbocyanine dyes, quinocarbocyanine dyes, quinothiacarbocyanine dyes, selenacarbocyanine dyes, imidacarbocyanine dyes, and oxacarbocyanine dyes.
- the substituent may be alone or a combination of two or more.
- substituents examples include an alkyl group, an alkoxy group, a hydroxyl group, a carboxyl group, a halogen atom, an allyl group, an alkylcarboxyl group, an alkylalkoxy group, an aralkyl group, an alkylcarbonyl group, a sulfonate alkyl group bound with a metal ion, a nitro group, an amino group, an alkyl amino group, an aryl group, and phenyl ethylene group.
- preferable examples include 1,3,3,1',3',3'-hexamethyl-2,2'-(4,5,4',5'-dibenzo)indocarbocyanine perchlorate, 3,3'-diethyl-2,2'-(6,7,6',7'-dibenzo) thiacarbocyanineiodide, 3,3'-diethyl-2,2'-thiacarbocyanine iodide, 1,1'-diethyl-2,2'-quinocarbocyanine iodide, 3,3'-diethyl-2,2'-selenacarbocyanine iodide, 1,3'-diethyl-4,2'-quinooxacarbocyanine iodide, 3,3',9-triethyl-2,2'-(4,5,4'5'-dibenzo)thiacarbocyanine bromide, 1,1'-diethyl-2,4'-
- the medium (b) has a dye-containing recording layer, an interference layer, and a reflective layer laminated in this order on a transparent substrate or has an interference layer, a dye-containing recording layer, and a reflective layer laminated in this order on the transparent substrate.
- the transparent substrate may be the same as the one used in the above mentioned medium (a).
- Optical characteristics of the dye-containing recording layer in the above mentioned medium (b) preferably hold the following relationships in respect to reflectance, recording sensitivity, and a degree of modulation: n1' ⁇ 1.8, 0.04 ⁇ k1' ⁇ 0.15, n2' ⁇ 1.1, and 0.04 ⁇ k2' ⁇ 0.6, where n1' is a value of the real part of the complex refractive index of the recording layer to a light beam having a wavelength of ⁇ 1, k1' is an absolute value of the imaginary part of the complex refractive index of the recording layer to a light beam of ⁇ 1, n2' is a value of the real part of the complex refractive index of the recording layer to a light beam having a wavelength of ⁇ 2, and k2' is an absolute value of the imaginary part of the complex refractive index of the recording layer to a light beam of ⁇ 2.
- n1' When n1' is smaller than 1.8 or when k1' is larger than 0.15, it becomes difficult to achieve the reflectance of 65% or higher to the light beam of ⁇ 1. On the contrary, k1' smaller than 0.04 deteriorates the recording sensitivity to the light beam of ⁇ 1.
- n2' smaller than 1.1 and k2' larger than 0.46 are not preferable in that they cause the reflectance to the light beam of ⁇ 2 to be lower than 15%.
- k2' There is no limitation on the minimum value of k2'. However, it is preferable that k2' is 0.04 or larger in respect to the recording sensitivity to the light beam of ⁇ 2 because it is desirable that the light beam of ⁇ 2 can be used for recording.
- a dye used in the recording layer of the medium (b) may be any one of adequate dyes as long as the optical constants (n1', k1', n2', and k2') of the recording layer are in the above mentioned range.
- the dye include phthalocyanine dyes, polymethine dyes, cyanine dyes, azo dyes, and naphthoquinone dyes.
- the phthalocyanine dyes are preferable in respect to light resistance and durability of the dyes.
- a phthalocyanine dye represented by the general formula (1) is most preferable in respect to the above mentioned optical constants and the recording sensitivity of the recording layer, and recording characteristics such as a degree of modulation, deformation of a reproduced waveform, an error rate, and a jitter value: wherein M is two hydrogen atoms, metals, metal oxides, or metal halides; Y1, Y2, Y3, and Y4 each are oxygen or sulfur; Z1, Z2, Z3, and Z4 each are a hydrocarbon group having from 4 to 12 carbon atoms or a group having from 4 to 12 carbon atoms and one or more atoms of at least one element selected from the group consisting of oxygen, nitrogen, sulfur and halogen; X1, X2, X3, and X4 each are a halogen, 11, l2, l3, and l4 each are 1 or 2; and m1, m2, m3, and m4 are each an integer of from 0 to 3.
- M of the phthalocyanine dye represented by the above general formula (1) include divalent metals such as Cu, Pd, Ni, Mg, Zn, Pb, and Cd; metal oxides such as VO; and metal halide such as AlCl.
- Z1, Z2, Z3, and Z4 each are a non-substituted or substituted hydrocarbon group having from 4 to 12 carbon atoms.
- saturated hydrocarbons such as a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, a dodecyl group, a cyclohexyl group, and a dimethylcyclohexyl group; and unsaturated hydrocarbon groups such as a butenyl group, a hexenyl group, an octenyl group, a dodecenyl group, a phenyl group, a methylphenyl group, a butylphenyl group, and a hexylphenyl group.
- hydrocarbons may be linear or branched.
- these hydrocarbons may be substituted by a halogen, an amino group, or an ether group. Even in the case where the hydrocarbon is substituted by amino or ether groups, the total number of carbons in Z1 through Z4 is from 4 to 12.
- the halogen represented by X1, X2, X3, and X4 may be, for example, fluorine, chlorine, bromine, and iodine.
- phthalocyanine dyes are as follows: More specifically, examples of the phthalocyanine dyes are those disclosed in U.S. Patent No. 5,124,067, which is hereby incorporated by reference.
- the film thickness of the interference layer affects not only the reflectance but also the recording characteristics such as the degree of modulation and the recording sensitivity.
- the film thickness of the interference layer depends on the material used therefor ranging from 30 - 500nm, preferably 50 - 300nm.
- the refractive index of the interference layer is ni and the film thickness is di (nm)
- ni x di is in a range from 100 to 300 to the light beams having the wavelengths of ⁇ 1 and ⁇ 2, respectively.
- the ni x di is smaller than 100, the reflectance to the light beam having the wavelength of ⁇ 2 becomes lower than 15% and the degree of modulation is small.
- the ni x di is larger than 300, the reflectance to the light beam having the wavelength of ⁇ 1 becomes lower than 65% and the recording sensitivity may sometimes be deteriorated depending on the type of the material used for the interference layer.
- the material used for the interference layer may be, for example, an inorganic dielectric, a polymer, or a dye. More specifically, the inorganic dielectric may be, for example, an oxide or a nitride of Si, Al, Ti, Ta, Zr, Sc, Hf, and Y and others; or a sulfide of Zn, Cd, and Sn and others. These materials may be used alone. Alternatively, a combination of a plurality of these materials may be employed.
- the polymer may be, for example, a thermoplastic resin or a thermosetting resin.
- Specific examples of the polymer include acrylic resins, polyvinyl acetate resins, vinylpyrrolidone resins, vinyl alcohol resins, butyral resins, formal resins, cellulose resins, silicone resins, polysiloxane resins, phenol resins, and polyimide resins, and copolymers thereof.
- the above mentioned inorganic dielectric and polymer are normally transparent to the light beams of ⁇ 1 and ⁇ 2, and have a similar refractive index.
- the light absorption characteristics and the refractive index to the light beams of ⁇ 1 and ⁇ 2 are different from dye to dye when a dye or dyes are used for the interference layer. It is apparent that the value of ni x di should meet the above mentioned conditions to the light beams of different wavelengths of ⁇ 1 and ⁇ 2, wherein ni represents a value of the real part of the complex refractive index.
- the light absorption characteristics are also important to take the possible effect of the present invention. An excessively large absorbance prevents the interference layer from having a desired reflectance. Considering the reflectance, it is preferable that the absolute value of the imaginary part of the complex refractive index of the dye is 0.15 or smaller to the light beam of ⁇ 1 and is 0.2 or smaller to the light beam of ⁇ 2.
- the dye used it is preferable to use the one having the maximum absorbance at shorter wavelength than 630 nm, and having a high refractive index at from 630 to 830 nm and a smaller absorbance at that wavelength range.
- Specific examples of such dye include cyanine dyes, squarylium dyes, azo dyes, porphyrin dyes, and tetra-azaporphyrin dyes. Of these, the azo dyes are preferable in respect to facility of film preparation and durability.
- the azo dye which may be a mixture of two or more dyes, represented by the following general formula (2) or a metal complex of that azo dye are most preferable in respect to recording characteristics such as a degree of modulation, deformation of a reproduced waveform, an error rate, and jitter value: wherein A is a residue forming a heterocyclic ring along with the nitrogen and carbon atoms bonded therewith; B is a residue forming an aromatic ring along with two carbon atoms bonded therewith; and X is a group having an active hydrogen.
- the residue forming the heterocyclic ring represented by A in the azo dye of the above general formula (2) may be, for example, a thiazole ring, a benzothiazole ring, a pyridobenzothiazole ring, a benzopyridothiazole ring, a pyridothiazole ring, a pyridine ring, and a quinoline ring. It is preferable that this residue is either the pyridine ring or the thiazole ring.
- These heterocyclic rings preferably have one or more substituents.
- substituents include an alkyl group, an alkyl halide group, an aryl group, an alkoxy group, an alkoxy halide group, an aryloxy group, an alkylthio group, an alkylthio halide group, an arylthio group, an aralkyl group, a halogen atom, a cyano group, a nitro group, an ester group, a carbamoyl group, an acyl group, an acylamino group, a sulfamoyl group, a sulfonamide group, an amino group, a hydroxyl group, a phenylazo group, a pyridinoazo group, and a vinyl group.
- substituents may optionally have a substituent or substituents.
- substituents for the heterocyclic ring include: an alkyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a fluoroalkyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, an alkoxy group having from 1 to 25 carbon atoms and optionally having a substituent or substituents, a halogen atom, a cyano group, a nitro group, an alkylthio group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a fluoroalkylthio group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, an alkylsulfamoyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a phenylsulfamoyl group having from 6 to 20 carbon
- Examples of the residue forming the aromatic ring represented by B in the general formula (2) include a benzene ring, a naphthalene ring, a pyridone ring, a pyridine ring, and a pyrazole ring. It is preferable that the aromatic ring is a benzene ring, and particularly the benzene ring substituted by at least one electron donating group.
- substituents include an alkyl group, an alkyl halide group, an aryl group, an alkoxy group, an alkoxy halide group, an aryloxy group, an alkylthio group, an alkylthio halide group, an arylthio group, an aralkyl group, a halogen atom, a cyano group, a nitro group, an ester group, a carbamoyl group, an acyl group, an acylamino group, a sulfamoyl group, a sulfonamide group, an amino group, a hydroxyl group, a phenylazo group, a pyridinoazo group, and a vinyl group.
- substituents optionally have a substituent or substituents.
- substituent for the aromatic ring include an alkyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a fluoroalkyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, and alkoxy group having from 1 to 25 carbon atoms and optionally having a substituent or substituents, a halogen atom, a cyano group, a nitro group, an alkylthio group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a fluoroalkylthio group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, an alkylsulfamoyl group having from 1 to 15 carbon atoms and optionally having a substituent or substituents, a phenylsulfamoyl group having from 6 to 20 carbon atoms
- the electron donating group include a monoalkylamino group having from 1 to 8 carbon atoms and optionally having a substituent or substituents, a dialkylamino group having from 2 to 8 carbon atoms and optionally having a substituent or substituents, an alkoxy group having from 1 to 8 carbon atoms and optionally having a substituent or substituents, an alkyl group having from 1 to 8 carbon atoms and optionally having a substituent or substituents, an aryloxy group having from 6 to 12 carbon atoms and optionally having a substituent or substituents, an aralkyl group having from 7 to 12 carbon atoms and optionally having a substituent or substituents, a carbamoyl group, an amino group, and a hydroxyl group.
- the above mentioned alkyl moiety may be sulfonated, nitrated, cyanated, halogenated, acetylated, or hydroxylated.
- the group X of the azo dye represented by the general formula (2) may be any group and is not limited to a specific one as long as it has an active hydrogen.
- Preferable examples of the group X include -OH, -COOH, - SO3H, -B(OH)2, -NHSO2R5 (R5 is a hydrogen atom, an alkyl group having from 1 to 25 carbon atoms and optionally having a substituent or substituents, or a phenyl group optionally having a substituent or substituents), -CONH2, -SO2NH2, and - NH2.
- Particularly preferable groups are -OH, -COOH, -SO3H, and -NHSO2R5 (R5 is the same as above).
- X is a group to be dissociative into an anion such as -OH, -COOH and -SO3H
- this group may be used as a salt with a cation, while it may be used as it is, to form an azo metal complex compound.
- the cation applicable include inorganic cations such as Na+, Li+, and K+, and organic cations such as P+(C6H5)4, N+(C2H5)4, N+(C4H9)4, and C6H5N+(CH3)3.
- the above mentioned azo dyes are used in the form of a metal complex.
- the metal having a capability of forming a complex with the azo dye may preferably be, for example, transition metals such as Ni, Co, Fe, Ru, Rh, Pd, Cu, Os, Ir, and Pt. Of these, Ni, Co, Cu, and Pd are particularly preferable.
- These metals are used in the form of acetate, halide, or BF4 ⁇ salt, and are coordinated as a complex with an azo compound in the form of Ni2+, Co2+, Co3+, Cu2+, and Pd2+.
- the azo-metal complex compound may be used alone. Alternatively, a combination of two or more such compounds may be employed.
- the metal complex of the azo dye used in the present invention may be synthesized according to a method disclosed in, for example, "Analytica Chemica Acta 140" (1982), by Furukawa, pages 281-289.
- metal complex of the azo compound used in the present invention include metal complex compounds of Ni2+, Co2+, Co3+, Cu2+, and Pd2+ etc with azo dyes such as: Specific examples of these compounds are those disclosed in Japanese Patent Publication No. 5-67438 and Table 1-9 of International Patent Laid-Open No. WO91/18950, which is hereby incorporated by reference.
- the recording layer is deposited on a transparent substrate.
- the deposition of the recording layer may be achieved through any one of adequate methods including spin coating, dip coating, spray coating, and vacuum deposition. Of these, the spin coating is preferable in respect to its simplicity.
- the solvent may preferably be a non-polar solvent or a polar solvent.
- the non-polar solvent include aliphatic or alicyclic hydrocarbon solvents such as hexane, heptane, octane, methylcyclohexane, ethylcyclohexane, dimethylcyclohexane, trimethylcyclohexane, propylcyclohexane, and cyclooctane, and ether solvents such as dipropylether and dibuthylether.
- polar solvent examples include alcohol solvents such as ethyl alcohol, propyl alcohol, butyl alcohol, furfuryl alcohol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, and tetrafluoropropanol.
- alcohol solvents such as ethyl alcohol, propyl alcohol, butyl alcohol, furfuryl alcohol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, and tetrafluoropropanol.
- these solvents may be mixed with aromatic hydrocarbons such as toluene, xylene, and propylbenzene, ester solvents such as ethyl acetate, butyl acetate, amyl acetate, and ethylene glycol monoethyl ether acetate, ketone solvents such as methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone, halogen-containing solvents such as chloroform, carbon tetrachloride, and methyl chloroform, and ether solvents such as dioxane, and tetrahydrofuran, in an amount not causing a damage to the substrate.
- aromatic hydrocarbons such as toluene, xylene, and propylbenzene
- ester solvents such as ethyl acetate, butyl acetate, amyl acetate, and ethylene glycol monoethyl ether acetate
- each group represented by Z1, Z2, Z3, and Z4 of the phthalocyanine dye having the above general formula (1) is a group having from 6 to 12 carbon atoms.
- the recording layer may be heated to dry the solvent after being deposited on the substrate through the spin coating.
- the dye may be added with, if necessary, additives such as quenchers, thermal decomposition promoters for the dye, ultraviolet absorbers, and adhesive. Alternatively, a substituent having such functions may be introduced into the dyes.
- the quencher include metal complexes based on acetyl acetonate, bisdithiol such as bisdithio- ⁇ -diketone, and bisphenyldithiol, thiocatechol, salicylaldehyde oxime, and thiobisphenolate.
- metal complexes based on acetyl acetonate bisdithiol such as bisdithio- ⁇ -diketone, and bisphenyldithiol, thiocatechol, salicylaldehyde oxime, and thiobisphenolate.
- amine-based complexes may also be used preferably.
- thermal decomposition promoter there is no specific limitation on the thermal decomposition promoter as long as promotion of thermal decomposition of the dye can be determined by means of thermogravimetric analysis (TG analysis).
- the thermal decomposition promoter may be, for example, a metal compound such as a metallic anti-knocking agent, a metallocene compound, and an acetylacetonato metal complex.
- a binder may be added thereto, if necessary.
- the binder include nitrocellulose, cellulose acetate, ketone resins, acrylic resins, poly(vinyl buthyral), polycarbonate, and polyolefin.
- a dye or dyes other than those described above may be added to the recording layer in order to improve the recording characteristics.
- the dyes may preferably be coated through the following method. More specifically, the light absorbing dye is dissolved into a solvent at a rate of 0.05 to 30% by weight, preferably 0.5 to 20% by weight. The resultant solution is coated with a spin coater.
- a film thickness of the recording layer is from 70 to 300 nm, and preferably from 80 to 250 nm, considering the degree of modulation and the reflectance. It is apparent that the excessively small film thickness inherently causes thermal radiation to a metal reflective layer described below, sometimes causing deterioration of the sensitivity.
- the film thickness is determined such that the recording layer has a proper absorbance to the light beams having the selected wavelengths of from 630 to 690 nm and from 770 to 830 nm.
- a layer of an inorganic compound or of a polymer may be provided on the substrate to improve chemical resistance, reflectance, and recording sensitivity of the substrate.
- the interference layer according to the present invention may be deposited through, for example, spin coating, dip coating, spray coating, vacuum deposition, or sputtering.
- the solvent may preferably be a non-polar solvent or a polar solvent. Specific examples of the solvent are as same as those described in conjunction with the recording layer.
- two layers i.e., the recording layer and the interference layer, may be deposited through spin coating.
- a polar solvent is used for the deposition of the interference layer when a non-polar solvent is used for the deposition of the recording layer.
- the interference layer is deposited with a non-polar solvent.
- additives such as quenchers, ultraviolet absorbers, and adhesives may be used if necessary.
- a substituent having such functions may be introduced into the dyes.
- a reflective layer is provided on the recording layer for the medium (a) and on either the interference layer or the recording layer for the medium (b).
- the reflective layer may be deposited through, for example, vacuum deposition or sputtering.
- the material of the reflective layer include metals having a high reflectance to the light beams of ⁇ 1 and ⁇ 2.
- the material may be, for example, metals such as Au, Ag, Al, Cu, and Pt and alloys containing these metals. Of these, gold is preferable in respect to the reflectance and the durability. Of course, other metal or metals may be added thereto in a small amount. An amount of other metals added is 10% or less, preferably 5% or less, and more preferably 2% or less.
- the film thickness of the reflective layer is typically from 40 to 300 nm, and preferably from 60 to 200 nm.
- a protective layer may be provided on the reflective layer or two media may be adhered to each other to protect the reflective layer.
- the protective layer may be formed through, as for the recording layer, coating such as spin coating and casting, sputtering, or chemical vapor deposition. Alternatively, a film or a substrate may be adhered. Of these methods, the spin coating is preferable.
- a material of the protective layer is not limited to a specific one as long as it can protect the reflective layer from an external force.
- organic compounds to be applicable as the protective layer include thermoplastic resins, thermosetting resins, and ultraviolet curing resins. Of these, the ultraviolet curing resins are preferable.
- the protective layer may be formed of an inorganic material. Examples of such inorganic materials include SiO2, SiN4, MgF2, and SnO2.
- the thermoplastic resins and the thermosetting resins may be dissolved into an adequate solvent to prepare a coating solution, which is then applied to the reflective layer and dried thereon as a protective layer.
- the ultraviolet curing resins may be as it is or dissolved into an adequate solvent to prepare a coating solution.
- This coating solution is then applied to the reflective layer, to which an ultraviolet ray is irradiated to cure the resin, thereby forming the protective layer.
- the ultraviolet resin include acrylate resins such as urethane acrylate, epoxy acrylate, polyester acrylate and epoxy resins.
- silicone-based hard coating resin may be used. These resins may be used alone or in the form of a mixture. Further, the resin may be laminated into a multi-layer structure rather than a single layer of the film.
- an ultraviolet curing resin or an inorganic thin film may be formed on a mirror-surface side of the substrate to protect the surface and to prevent adhesion of dust.
- the optical recording medium according to the present invention so obtained may be recorded or played back by means of focusing a laser beam onto the recording layer.
- a signal used upon recording may be, for example, an EFM modulated signal used for CDs.
- the medium according to the present invention has a recording layer with the dye having absorption at a wavelength of around 770 to 830 nm. In this medium, the reflectance of 65% or higher can be achieved to the light beam having the selected wavelength of from 770 to 830.
- the information can thus be recorded and reproduced with a laser beam having a wavelength of around 780 nm.
- the recorded information may be reproduced by using a commercially available CD or CD-ROM player. The characteristics of the reproduced signal well satisfy the CD-R standards, or the Orange Book Standards.
- the reflectance of 15% or higher can be achieved to the light beam having a selected wavelength of from 630 to 690 nm.
- the information on the medium of the present invention may thus be reproduced by using a player for high-density, in which a laser of a selected wavelength of from 630 to 690 nm is mounted.
- the light beam used for the players for high-density has a wavelength of from 630 to 690 nm
- a laser used for practical applications have a wavelength of, for example, around 635 nm, 650 nm or 680 nm.
- the medium according to the present invention has absorption at 630 to 690 nm, so that information can be recorded thereon by using a light beam having a selected wavelength of from 630 to 690 nm.
- a dye to form a recording layer As a dye to form a recording layer, 0.2 g of trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (3) and 0.01 g of pentamethine cyanine dye NK2929 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (4) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- trimethine cyanine dye NK3239 produced by Nippon Kanko Shikiso Kenkyusho KK
- pentamethine cyanine dye NK2929 produced by Nippon Kanko Shikiso Kenkyusho KK
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 130 nm, a width of 0.5 ⁇ m, and a pitch of 1.6 ⁇ m.
- the dye solution was coated on the surface of the substrate by spin coating at a rotation rate of 1200 rpm to form a layer. This layer was dried at 70°C for 2 hours to provide a recording layer having a film thickness of approximately 150 nm.
- the refractive index (the value of the real part of the complex refractive index) was 2.1
- the attenuation coefficient (the absolute value of the imaginary part of the complex refractive index) was 0.08 at the wavelength of 780 nm.
- the refractive index and the attenuation coefficient were 2.0 and 0.17, respectively, at 680 nm while the refractive index and the attenuation coefficient were 2.5 and 0.26, respectively, at 635 nm.
- the refractive index and the attenuation coefficient of the recording layer were measured and calculated after coating the same dye solution on a glass substrate by spin coating.
- an Au film was formed by sputtering on this recording layer by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer of 80 nm thick.
- Sputtering conditions were as follows: Sputtering power; 2.5 kW Sputtering gas (argon gas) pressure; 1.0 x 10 ⁇ 2 Torr.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective film of 6 ⁇ m in thickness.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 8 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 680 nm and a CD encoder (available from KENWOOD).
- the recorded signal was reproduced at a linear speed of 1.4 m/sec by using the same estimation device.
- the reflectance was 58% and the error rate was less than 5 cps, when measured by using a CD decoder DR3552 (available from KENWOOD).
- the degree of modulation of the shortest pit (I3/Itop) was 0.45.
- Jitter value was measured by using a jitter meter LJM-1851 (available from Leader Electronics Corp.). The result was good.
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser capable of providing a reproducing wavelength of 780 nm.
- an optical disc estimation device available from Pulstec Industrial Co., Ltd.
- the reflectance was 70%
- the error rate was less than 5 cps
- I3/Itop was 0.50.
- the reproduced signal had small deformation in waveform, and the jitter value was good to satisfy the Orange Book Standards.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 10 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a CD encoder (available from KENWOOD).
- the recorded signal was reproduced by using a commercially available CD player CDX-1050 (available from YAMAHA) having a reproducing wavelength of 786 nm.
- CDX-1050 available from YAMAHA
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec. by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser for a red semiconductor laser capable of providing a reproducing wavelength of 680 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 58%
- the error rate was less than 5 cps
- I3/Itop was 0.47.
- the jitter value was good.
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser capable of providing a reproducing wavelength of 635 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 28%
- the error rate was less than 5 cps
- I3/Itop was 0.50.
- the jitter value was good.
- the spectral absorption maximum of the dye used was measured by means of coating the dye solution on a glass substrate by spin coating, and drying it at 70°C for 2 hours to form a thin film of the dye. The film was then subjected to measurement by using an ultraviolet-visible ray spectrophotometer UV-2200 (available from Shimadzu Corporation). As a result, the spectral absorption maximum of NK3239 was 590 nm and that of NK2929 was 730 nm.
- Example 1 was repeated to produce a medium except that 0.2 g of trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3) and 0.046 g of pentamethine cyanine dye NK2929 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (4) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- trimethine cyanine dye NK3239 produced by Nippon Kanko Shikiso Kenkyusho KK
- pentamethine cyanine dye NK2929 produced by Nippon Kanko Shikiso Kenkyusho KK
- Example 2 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3)
- pentamethine cyanine dye NK2929 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (4)
- heptamethine cyanine dye NK2014 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (5) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol(produced by Tokyo Kasei KK).
- a recording layer of 150 nm thick was then formed in the same manner as in Example 1. Then, an Au film was formed by sputtering on this recording layer by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer of 100 nm thick.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective film of 5 ⁇ m in thickness.
- Example 2 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 1 was repeated to produce an optical recording medium except that 0.2 g of trimethine cyanine dye NK467 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (6), 0.01 g of pentamethine cyanine dye NK2627 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (7), and 0.01 g of heptamethine cyanine dye NK2014 (produce d by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (5) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 1 was repeated to produce an optical recording medium except that 0.2 g of trimethine cyanine dye NK3 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (8), 0.01 g of pentamethine cyanine dye NK1456 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (9), and 0.01 g of heptamethine cyanine dye NK2014 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (5) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 1 was repeated to produce an optical recording medium except that 0.2 g of trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3), 0.025 g of pentamethine cyanine dye NK1456 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (9), and 0.01 g of heptamethine cyanine dye NK1666 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (10) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 1 was repeated to produce an optical recording medium except that 0.2 g of trimethine cyanine dye NK3 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (8), 0.01 g of pentamethine cyanine dye NK2627 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (7), and 0.025 g of heptamethine cyanine dye NK1666 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (10) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- trimethine cyanine dye NK3 produced by Nippon Kanko Shikiso Kenkyusho KK
- pentamethine cyanine dye NK2627 produced by Nippon Kanko Shikiso
- Example 2 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 1 was repeated to produce an optical recording medium except that the dye used was only the trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3).
- the dye used was only the trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3).
- Example 2 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, it was impossible to record a signal with the wavelength of 780 nm.
- the refractive index and the attenuation coefficient of the recording layer were measured in the same manner as in Example 1.
- Example 1 was repeated to produce an optical recording medium except that 0.14 g of trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3), and 0.06 g of pentamethine cyanine dye NK2929 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (4) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution, and that a mixing ratio of pentamethine cyanine dye to trimethine cyanine dye in the dye solution was increased from 5% in Example 1 to 30%.
- trimethine cyanine dye NK3239 produced by Nippon Kanko Shikiso Kenkyusho KK
- pentamethine cyanine dye NK2929 produced by Nippon Kanko Shikiso Kenkyusho KK
- Example 1 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, no satisfactory reproduction signal was obtained at each wavelength.
- the refractive index and the attenuation coefficient of the recording layer were measured in the same manner as in Example 1.
- Example 1 was repeated to produce an optical recording medium except that 0.1 g of trimethine cyanine dye NK3239 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (3), and 0.1 g of heptamethine cyanine dye NK2014 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (5) were dissolved into 10 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- trimethine cyanine dye NK3239 produced by Nippon Kanko Shikiso Kenkyusho KK
- heptamethine cyanine dye NK2014 produced by Nippon Kanko Shikiso Kenkyusho KK
- Example 1 For the medium obtained, the recording and reproduction tests were made as in Example 1. As a result, no satisfactory reproduction signal was obtained at each wavelength.
- the refractive index and the attenuation coefficient of the recording layer were measured in the same manner as in Example 1.
- Table 1 shows the spectral absorption maximum ( ⁇ max) of the dyes, the mixing weight ratio (%) of the dyes in the recording layers, and the optical constants (refractive index (n) and attenuation coefficient (k)) of the recording layers obtained at each wavelength in Examples 1 through 7 and Comparative Examples 1 through 3.
- Table 2 shows characteristics (reflectance, error rate, and degree of modulation of the shortest pit) of the reproduced signal obtained at each wavelength.
- a dye to form a recording layer As a dye to form a recording layer, 2.2 g of trimethine cyanine dye NK737 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (11) and 0.4 g of phthalocyanine dye (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the following formula (12) were dissolved into 100 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution.
- trimethine cyanine dye NK737 produced by Nippon Kanko Shikiso Kenkyusho KK
- phthalocyanine dye produced by Nippon Kanko Shikiso Kenkyusho KK
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 130 nm, a width of 0.5 ⁇ m, and a pitch of 1.6 ⁇ m.
- the dye solution was coated on the surface of the substrate by spin coating at a rotation rate of 1600 rpm to form a layer. This layer was dried at 70°C for 2 hours to provide a recording layer.
- the absorbance of this recording layer were 0.35, 0.27, and 0.23 at the wavelength of 635 nm, 680 nm, and 780 nm, respectively.
- the spectral absorption maximum and the absorbance, at each wavelength, of the recording layer were measured by means of coating the dye solution on a glass substrate by spin coating, and drying it at 70°C for 2 hours to form a thin film of the dye. The film was then subjected to measurement by using an ultraviolet-visible ray spectrophotometer UV-2200 (available from Shimadzu). The absorbance is a value obtained by taking off the absorption by the substrate.
- an Au film was formed by sputtering on this recording layer by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer of 80 nm thick.
- Sputtering conditions were as follows: Sputtering power; 2.5 kW Sputtering gas (argon gas) pressure; 1.0 x 10 ⁇ 2 Torr.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective film of 6 ⁇ m in thickness.
- a laser was irradiated at a linear speed of 4.8 m/sec. with a recording power of 10 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 680 nm and a CD encoder (available from KENWOOD).
- the recorded signal was reproduced by using the same estimation device.
- the reflectance was 32% and the error rate was less than 5 cps, when measured by using a CD decoder DR3552 (available from KENWOOD).
- the degree of modulation of the shortest pit (I3/Itop) was 0.43.
- Jitter value was measured by using a jitter meter LJM-1851 (available from Leader Electronics Corp.). The result was good.
- the recorded sample was subjected to a reproduction estimation by using an optical disc estimation device (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser capable of providing a reproducing wavelength of 780 nm.
- an optical disc estimation device available from Pulstec Industrial Co., Ltd.
- the reflectance was 66%
- the error rate was less than 5 cps
- I3/Itop was 0.45.
- the signal had small deformation in waveform, and the jitter value was good to satisfy the Orange Book Standards.
- a laser was irradiated at a linear speed of 1.4 m/sec. with a recording power of 8 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a CD encoder (available from KENWOOD).
- the recorded signal was reproduced by using a commercially available CD player CDX-1050 (available from YAMAHA) having a reproducing wavelength of 786 nm.
- CDX-1050 available from YAMAHA
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser capable of providing a reproducing wavelength of 680 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 31%
- the error rate was less than 5 cps
- I3/Itop was 0.43.
- the jitter value was good.
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser capable of providing a reproducing wavelength of 635 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 20%
- the error rate was less than 5 cps
- I3/Itop was 0.45.
- the jitter value was good.
- the spectral absorption maximum of the dye used was measured by means of coating the dye solution on a glass substrate by spin coating, and drying it at 70°C for 2 hours to form a thin film of the dye. The film was then subjected to measurement by using an ultraviolet-visible ray spectrophotometer UV-2200 (available from Shimadzu Corporation). As a result, the spectral absorption maximum of NK737 was 570 nm and that of the phthalocyanine dye represented by the formula (12) was 745 nm.
- Example 8 was repeated to produce a medium except that 3.0 g of porphyrin represented by the following formula (13) and 0.5 g of pentamethine cyanine dye NK2929 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (4) were dissolved into 100 ml of 2,2,3,3-tetrafluoro-1-propanol to prepare a dye solution, which was then coated by spin coating. To the medium obtained, a laser was irradiated at a linear speed of 2.4 m/sec.
- Example 8 For the medium obtained, the recording and reproduction tests were made as in Example 8. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 8 was repeated to produce an optical recording medium except that 3.0 g of anthraquinone dye represented by the following formula (14) was used in place of trimethine cyanine dye NK737 (produced by Nippon Kanko Shikiso Kenkyusho KK) represented by the above formula (11).
- a laser was irradiated at a linear speed of 2.4 m/sec. with a recording power of 8 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 680 nm and a pulse generator (available from KENWOOD).
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- a pulse generator available from KENWOOD
- a laser was irradiated at a linear speed of 2.4 m/sec. with a recording power of 7.5 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a pulse generator (available from KENWOOD).
- the recorded medium was subjected to reproduction estimation in the same manner as in Example 8.
- the reproduced signal had small deformation in waveform, which satisfied the Orange Book Standards.
- the absorbance of the recording layer at each wavelength was also measured in the same manner as in Example 8.
- Example 8 was repeated to produce a medium except that 2.8 g of azo dye represented by the following formula (15) and 0.65 g of phthalocyanine dye represented by the following formula (16) were dissolved into 100 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution, which was then coated by spin coating at 1600 rpm.
- the recording and reproduction tests were made as in Example 8. As a result, the reflectance, the degree of modulation, the error rate, and the jitter value were all good at each wavelength.
- Example 8 was repeated to produce a medium except that 2.3 g of tetraazaporphyrin dye represented by the following formula (17) and 0.4 g of phthalocyanine dye represented by the above formula (16) were dissolved into 100 ml of 2,2,3,3-tetrafluoro-1-propanol (produced by Tokyo Kasei KK) to prepare a dye solution, which was then coated by spin coating at 1600 rpm. To the medium obtained, a laser was irradiated at a linear speed of 2.4 m/sec.
- a laser was irradiated at a linear speed of 1.2 m/sec. with a recording power of 7.0 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a pulse generator (available from KENWOOD).
- the recorded medium was subjected to reproduction estimation in the same manner as in Example 8.
- the reproduced signal had small deformation in waveform, which satisfied the Orange Book Standards.
- the absorbance of the recording layer at each wavelength was also measured in the same manner as in Example 8.
- Example 8 was repeated to produce an optical recording medium except that the dye used was 2.6 g of phthalocyanine dye alone which is represented by the above formula (12).
- Example 8 For the medium obtained, the recording and reproduction tests were made as in Example 8. As a result, it was impossible to obtain good reproduction signal at each wavelength. In particular, the medium could not be played back by using a commercially available CD player having a reproduction wavelength of 786 nm.
- Example 9 was repeated to produce an optical recording medium except that the dye used was 3.0 g of porphyrin dye alone which is represented by the above formula (13).
- a laser was irradiated at a linear speed of 1.4 m/sec. with a recording power of 11 mW to record information by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a pulse generator (available from KENWOOD). As a result, it was impossible to record a signal at a wavelength of 780 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- a pulse generator available from KENWOOD
- Table 3 shows the spectral absorption maximum ( ⁇ max) of the dyes, the mixing weight ratio (%) of the dyes in the recording layers, and the absorbance of the recording layers at each wavelength in Examples 8 through 12 and Comparative Examples 4 and 5.
- Table 4 shows characteristics (reflectance, error rate, and degree of modulation) of the reproduced signal obtained at each wavelength.
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 140 nm, a width of 0.4 ⁇ m, and a pitch of 1.2 ⁇ m.
- the dye solution was coated on the surface of the substrate by spin coating at a rotation rate of 1600 rpm to form a layer.
- the absorbance of this recording layer were 0.22, 0.18, and 0.13 at the wavelength of 635 nm, 680 nm, and 780 nm, respectively.
- the spectral absorption maximum and the absorbance, at each wavelength, of the recording layer were measured by means of coating the dye solution on a glass substrate by spin coating, and drying it at 70°C for 2 hours to form a thin film of the dye.
- the film was then subjected to measurement by using an ultraviolet-visible ray spectrophotometer UV-2200 (available from Shimadzu).
- UV-2200 available from Shimadzu
- an Au film was formed by sputtering on this recording layer by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer of 80 nm thick.
- Sputtering conditions were as follows: Sputtering power; 2.5 kW Sputtering gas (argon gas) pressure; 1.0 x 10 ⁇ 2 Torr.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective film of 5 ⁇ m in thickness.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 9 mW to record EFM signals by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a near infrared semiconductor laser of 780 nm and a CD encoder (available from KENWOOD).
- the recorded signal was reproduced at a linear speed of 1.4 m/sec by using the same estimation device.
- the reflectance was 70% and the error rate was less than 5 cps, when measured by using a CD decoder DR3552 (available from KENWOOD).
- the degree of modulation of the shortest pit (I3/Itop) was 0.48.
- the jitter value was good to satisfy the Orange Book Standards.
- the reproduced waveform had less deformation.
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser capable of providing a reproducing wavelength of 635 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 30%
- the error rate was less than 5 cps
- I3/Itop was 0.50.
- the recording mode was high-to-low where the reflectance at the recording portion is reduced.
- the jitter value was very good.
- the recorded sample was subjected to a reproduction estimation at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser capable of providing a reproducing wavelength of 680 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 26%
- the error rate was less than 5 cps
- I3/Itop was 0.45.
- the recording mode was high-to-low where the reflectance at the recording portion is reduced.
- the jitter value was very good.
- the medium obtained was subjected to recording and reproduction by using drives having a semiconductor laser of 680 nm and a He-Ne laser of 630 nm, respectively. Good recording and reproduction were achieved. It was confirmed that a good reproduction signal can be obtained from the recorded medium by using a player at 780 nm.
- the spectral absorption maximum of the dye used was measured by means of coating the dye solution on a glass substrate by spin coating, and drying it at 70°C for 2 hours to form a thin film of the dye. The film was then subjected to measurement by using an ultraviolet-visible ray spectrophotometer UV-2200 (available from Shimadzu).
- UV-2200 ultraviolet-visible ray spectrophotometer
- Example 13 was repeated to produce a medium for estimation except that the dye used was a combination of metal complexes of the azo dyes having the absorption maximum at a wavelength shorter than 630 nm, which were represented by the formulae (18), and (20) through (23), and the dye having the absorption maximum at 630-900 nm represented by the formulae (19), and (24) through (26).
- Table 5 shows combinations of the dyes, the spectral absorption maximum ( ⁇ max) of each dye, the mixed weight ratio of the dyes (%), and the absorbance of the recording layer at each wavelength.
- a medium was produced with a Ni metal complex of the azo compound represented by the formula (18) and following pentamethine cyanine dye mixed at a weight ratio of 40:60.
- the medium was estimated in the same manner as in Example 13. Recording and reproduction at 780 nm were achieved well. However, reproduction at 635 nm provided the reflectance as small as 9%. In addition, the degree of modulation was too small to achieve reproduction.
- the spectral absorption maximum of the heptamethine cyanine dye in the form of a film was 690 nm. This dye has a large absorption at 600-720 nm.
- Comparative Example 6 was repeated to produce a medium except that the Ni metal complex of the azo compound and the pentamethine cyanine dye in Comparative Example 6 were mixed at a weight ratio of 25:75.
- a non-recorded portion had a reflectance of 30% at a wavelength of 635 nm, while less or no recording could be achieved at 780 nm even when the power was increased to 15 mW.
- Example 13 was repeated to produce a medium except that the Ni metal complex of the azo dye represented by the formula (18) and the heptamethinecyanine dye represented by the formula (19) were used at a varied mixing ratio.
- Table 5 shows the spectral absorption maximum ( ⁇ max) of each dye, the mixing weight ratio (%) of the dyes, and the absorbance of the recording layer at each wavelength.
- Table 6 shows characteristics (reflectance, error rate, and degree of modulation of the shortest pit) of the reproduced signals at 780 nm and 635 nm obtained in Examples 13 through 19 and Comparative Examples 6 through 9.
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 140 nm, a width of 0.4 ⁇ m, and a pitch of 1.6 ⁇ m.
- the dye solution was coated on the surface of the substrate by spin coating at a rotation rate of 1500 rpm to form a layer.
- This layer was dried at 70°C for 2 hours to provide a recording film of 120 nm.
- the refractive index and the attenuation coefficient were 2.0 and 0.05, respectively, at 780 nm, while the refractive index and the attenuation coefficient were 1.15 and 0.36 at 635 nm.
- an Si3N4 film (light interference layer) of 85nm thick was formed by means of reaction sputtering with a sputtering device CFS-4EP (available from Shibaura Engineering Works Co., Ltd.).
- the refractive index of this thin film was 1.84 at both wavelengths of 780 nm and 635 nm. Accordingly, the product of the refractive index and the film thickness (ni x di) of this interference layer at both wavelengths is equal to 156.
- an Au film of 100 nm thick was formed by sputtering on this Si3N4 film by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective layer of 6 ⁇ m in thickness. The optical recording medium was thus completed.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 8 mW to record EFM signals by using a writer CCD-521 (available from Phillips Co.) with a laser head for a semiconductor laser of 780 nm.
- the recorded signal was reproduced by using a commercially available CD player (YAMAHA CDX-1050; laser wavelength 786 nm) and the characteristics of the reproduced signal were estimated.
- the reflectance was 71%
- the error rate was less than 5 cps
- I3/Itop was 0.45.
- the recording mode was high-to-low, and the reproduced signal had less deformation.
- the jitter value was very good, and thus the Orange Book Standards was satisfied.
- the signal recorded by the writer (CDD-521) was reproduced and estimated at a linear speed of 1.4 m/sec by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 635 nm.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- the reflectance was 22%
- I3/Itop was 0.48.
- the reproduced signal had less deformation, and the jitter value as well as error rate were very good.
- Example 20 was repeated to produce a medium except that the dye used was Pd ⁇ phthalocyanine having one l-isopropyl-isoamyloxy group at ⁇ -positions of four benzene rings forming phthalocyanine with addition of 3.5 bromines on average per pd ⁇ phthalocyanine molecule, which is represented by the following formula (28), and that an AlN light interference layer of 100 nm was formed.
- the dye used was Pd ⁇ phthalocyanine having one l-isopropyl-isoamyloxy group at ⁇ -positions of four benzene rings forming phthalocyanine with addition of 3.5 bromines on average per pd ⁇ phthalocyanine molecule, which is represented by the following formula (28), and that an AlN light interference layer of 100 nm was formed.
- the optical constants of this recording film was as follows: the refractive index and the attenuation coefficient were 2.2 and 0.08, respectively, at 780 nm; the refractive index and the attenuation coefficient were 1.2 and 0.49, respectively, at 680 nm; and n and k were 1.2 and 0.34, respectively, at 635 nm.
- the refractive index of the light interference layer was 1.95 at the wavelengths of 780, 680, and 635 nm, while the product of the refractive index and the film thickness (ni x di) of the light interference layer at each wavelength was 195.
- this medium was subjected to recording and reproduction estimation with a laser power of 8 mW in the same manner as in Example 20. More specifically, the medium was reproduced by using a commercially available CD player. As a result, all characteristics satisfied the Orange Book Standards, providing good reproduction.
- the medium was also subjected to estimation by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a red semiconductor laser head for 635 nm. As a result, the reflectance was 25% and I3/Itop was 0.47. The reproduced signal had less deformation in waveform, and the jitter value as well as error rate were very good.
- the recorded sample was estimated by using the optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a red semiconductor laser head for 680 nm. As a result, the reflectance was 26%, the error rate was lower than 5 cps, and I3/Itop was 0.50 with the recording mode being high-to-low. The jitter value was very good.
- the medium obtained was subjected to recording and reproduction by using a drive with a semiconductor laser of 680 nm and a drive with a He-Ne laser of 630 nm. Satisfactory level of recording and reproduction were achieved with both drives. In addition, it was confirmed that the recorded medium can provide a good reproduction signal when played back by using a player for a wavelength of 780 nm.
- Example 20 was repeated to produce and estimate a medium except that the dye used in Example 20 was replaced with Ni ⁇ phthalocyanine dye having one octhylthio group at ⁇ -positions of four benzene rings forming phthalocyanine represented by the following formula (29), in which illustrated is a typical isomer though there are various isomers depending on combinations of ⁇ -position substituted by a substituent, and that a ZrO2 light interference layer of 105 nm was formed rather than the Si3N4 light interference layer.
- Ni ⁇ phthalocyanine dye having one octhylthio group at ⁇ -positions of four benzene rings forming phthalocyanine represented by the following formula (29), in which illustrated is a typical isomer though there are various isomers depending on combinations of ⁇ -position substituted by a substituent, and that a ZrO2 light interference layer of 105 nm was formed rather than the Si3N4 light interference layer.
- the refractive index and the attenuation coefficient were 2.3 and 0.12, respectively at 780 nm, while the refractive index and the attenuation coefficient were 1.2 and 0.30, respectively, at 635 nm.
- the refractive index of the light interference layer was 2.21 at both wavelengths, while the product of the refractive index and the film thickness (ni x di) of this interference layer at both wavelengths was 232.
- the signal was reproduced and estimated by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 635 nm. As a result, the reflectance was 27%, and I3/Itop was 0.50. The reproduced signal had less deformation, and the jitter value as well as error rate were very good.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- Example 20 was repeated to produce an optical recording medium except that the light interference layer was not provided thereon.
- An EFM signal was recorded on the medium obtained by using a writer available from Phillips Co. with a semiconductor laser head for 780 nm in the same manner as in Example 20.
- the recorded signal was reproduced for estimation by using a CDX-1050 with a semiconductor laser head for 786 nm and DDU-1000 with a semiconductor laser head for 635 nm.
- the CDX-1050 provided the reproduction that satisfied the Orange Book Standards.
- the reflectance was 10% or lower and no reproduced waveform was read with DDU-1000.
- Example 21 was repeated to produce two optical recording media except that the film thickness of the light interference layers were 45 nm and 165 nm, respectively.
- the product of the refractive index and the film thickness was 87.8 for the medium with the light interference layer of 45 nm thick.
- the reflectance was as low as 12% when reproduced by using an estimator mounting a laser of 635 nm. It was thus impossible to reproduce the recorded signal. In addition, the error rate and the jitter value were too large to prevent the reproduction.
- the product of the refractive index and the film thickness was 321.8 for the medium with the light interference layer of 165 nm thick. The reflectance and the degree of modulation were small so as not to satisfy the Orange Book Standards when reproduced by a commercially available CD player with recording laser power of 18 mW.
- Example 21 was repeated to produce a recording film by using the Pd ⁇ phthalocyanine dye represented by the formula (28).
- the recording layer had a film thickness of 150 nm.
- the optical constants of this recording layer were as follows: the refractive index and the attenuation coefficient were 2.2 and 0.08, respectively, with a light beam having a wavelength of 780 nm, and the refractive index and the attenuation coefficient were 1.2 and 0.49, respectively, with a light beam having a wavelength of 680 nm, and the refractive index and the attenuation coefficient were 1.2 and 0.34, respectively, with a light beam having a wavelength of 635 nm.
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 140 nm, a width of 0.4 ⁇ m, and a pitch of 1.2 ⁇ m.
- a 3%-methylcellosolve solution of vinylpyrrolidone-vinyl acetate copolymer resin was coated on the recording layer by spin coating as a light interference layer. This layer was dried at 70°C for 2 hours.
- the film thickness di of the light interference layer was 120 nm.
- the refractive index ni of this polymer was 1.45 for both the light beams having wavelengths of 780 nm and 635 nm, and ni x di was 174 for both wavelengths.
- an ultraviolet curing resin (SD-17, available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective layer of 5 ⁇ m in thickness and thereby produce an optical recording medium.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 8 mW to record EFM signals by using a writer CDD-521 (available from Phillips Co.) with a laser head for a semiconductor laser of 780 nm.
- the recorded signal was reproduced at a linear speed of 1.4 m/sec by using the same estimation device for estimation of the characteristics.
- the reflectance was 71% and the error rate was less than 5 cps.
- I3/Itop was 0.45.
- the recording mode was high-to-low mode and the reproduced signal had less deformation in waveform. The jitter value was very good and the Orange Book Standards was satisfied.
- the recorded medium was subjected to signal reproduction at a linear speed of 1.4 m/sec by using a player for high-density which has a semiconductor laser of 635 nm.
- the reflectance was 24% with a large degree of modulation.
- the recording mode was high-to-low recording at which the reflectance at the recorded portion is decreased.
- the error rate and the jitter value were small, providing good reproduction.
- the medium was played back by using a player having a semiconductor laser of 680 nm.
- the reflectance was 21%
- the recording mode was high-to-low recording with a large degree of modulation.
- the error rate and the jitter value were small, providing good reproduction.
- this medium permits good recording when a signal was recorded with the light beam of 680 nm at a linear speed of 8.4 m/sec. with a recording power of 8.0 mW.
- Example 23 was repeated to produce a medium except that the film thickness of the light interference layer was 160 nm.
- the product of the refractive index and the film thickness, i.e., ni x di, of the light interference layer was 232 for both wavelengths of 635 nm and 780 nm.
- this medium was subjected to recording and reproduction estimation in the same manner as in Example 23.
- the reflectance was 68%
- the error rate was less than 5 cps
- I3/Itop was 0.47 at 780 nm.
- the jitter value was small and the reproduced signal had less deformation in waveform, permitting good recording and reproduction.
- the signal recorded on this medium could readily be reproduced through a commercially available CD player.
- the reflectance when reproduced at 635 nm, the reflectance was 27%, the I3/Itop was 0.48, and the recording mode was high-to-low.
- the error rate and the jitter value were extremely small, permitting good reproduction.
- Example 23 was repeated to produce a medium except that the dye used was Cu ⁇ phthalocyanine dye having one l-isopropyl-isoamyloxy group at ⁇ -positions of four benzene rings forming phthalocyanine represented by the following formula (30), in which illustrated is a typical isomer though there are various isomers depending on combinations of ⁇ -positions substituted by a substituent, and that an alcohol solution of polysiloxane was used as the light interference layer having a film thickness di of 120 nm.
- the dye used was Cu ⁇ phthalocyanine dye having one l-isopropyl-isoamyloxy group at ⁇ -positions of four benzene rings forming phthalocyanine represented by the following formula (30), in which illustrated is a typical isomer though there are various isomers depending on combinations of ⁇ -positions substituted by a substituent, and that an alcohol solution of polysiloxane was used as the light interference layer having a film thickness di of 120 nm
- the refractive index and the attenuation coefficient were 2.0 and 0.06, respectively, with a light beam having a wavelength of 780 nm, while the refractive index and the attenuation coefficient were 1.2 and 0.30 with a light beam having a wavelength of 635 nm.
- the refractive index ni of the light interference layer was 1.40 for both wavelengths of 780 nm and 635 nm. Accordingly, the product of the refractive index and the film thickness (ni x di) of this interference layer at both wavelengths was 168.
- this medium was subjected to recording and reproduction estimation in the same manner as in Example 23.
- the reflectance was 67%
- the error rate was less than 5 cps
- I3/Itop was 0.43 at 780 nm.
- the jitter value was small and the reproduced signal had less deformation in waveform, permitting good recording and reproduction.
- the signal recorded on this medium could readily be reproduced through a commercially available CD player.
- the reflectance when reproduced at 635 nm, the reflectance was 30%, the I3/Itop was 0.47, and the recording mode was high-to-low.
- the error rate and the jitter value were extremely small, permitting good reproduction.
- Example 23 was repeated to produce a medium except that Ni ⁇ phthalocyanine dye represented by the above formula (29) was used.
- the refractive index and the attenuation coefficient were 2.3 and 0.12, respectively, with a light beam having a wavelength of 780 nm, while the refractive index and the attenuation coefficient were 1.2 and 0.30 with a light beam having a wavelength of 635 nm.
- This medium was subjected to recording and reproduction estimation in the same manner as in Example 23.
- the reflectance was 66%
- the error rate was less than 5 cps
- I3/Itop was 0.42 at 780 nm.
- the jitter value was small and the reproduced signal had less deformation in waveform, permitting good recording and reproduction.
- the signal recorded on this medium could readily be reproduced through a commercially available CD player.
- the reflectance when reproduced at 635 nm, the reflectance was 26%, the I3/Itop was 0.39, and the recording mode was high-to-low.
- the error rate and the jitter value were extremely small, permitting good reproduction.
- Example 23 was repeated to produce and estimate media with the light interference layers of 60 nm (Comparative Example 12) and 230 nm (Comparative Example 13) in thickness.
- the product of the refractive index and the film thickness i.e., ni x di
- the reflectance at the wavelength of 635 nm was 9%.
- the recording mode was low-to-high mode with a small degree of modulation. This medium thus could not be played back by a player for high density.
- the light interference layer of the medium according to Comparative Example 13 had ni x di of 334.
- the reflectance at the wavelength of 780 nm was 55%. This medium could not be played back by using a commercially available CD player.
- Example 23 was repeated to produce and estimate a medium having a recording layer of 160 nm thick by using a heptamethine cyanine dye NK3219 (Nippon Kanko Shikiso Kenkyusho KK) and a silicone resin light interference layer of 140 nm thick formed thereon.
- a heptamethine cyanine dye NK3219 Nippon Kanko Shikiso Kenkyusho KK
- silicone resin light interference layer 140 nm thick formed thereon.
- the refractive index was 2.6, and the attenuation coefficient was 0.11 at the wavelength of 780 nm.
- the refractive index and the attenuation coefficient were 1.9 and 1.31, respectively, at 680 nm while the refractive index and the attenuation coefficient were 1.09 and 1.21, respectively, at 635 nm.
- the refractive index of the light interference layer ni was 1.40 at each wavelength of 780 nm, 680 nm and 635 nm. Therefore the product of the refractive index and the film thickness (ni x di) was 196.
- this medium was subjected to recording and reproduction estimation in the same manner as in Example 23.
- the reflectance was 71%
- the error rate was less than 5 cps
- the degree of modulation was sufficiently large at 780 nm.
- the jitter value was small and the reproduced signal had less deformation in waveform, permitting good recording and reproduction.
- the recorded signal on this medium could readily be reproduced through a commercially available CD player.
- the medium recorded at 780 nm was reproduced at 680 nm and 635 nm
- the reflectance was 8% and 9%, respectively and the recording mode was low to high.
- the degree of modulation was low, and thus reproduction was difficult.
- a substrate used was a polycarbonate substrate of a disc shape having a thickness of 1.2 mm and a diameter of 120 mm ⁇ and having a spiral pre-groove formed on its surface with a depth of 170 nm, a width of 0.5 ⁇ m, and a pitch of 1.6 ⁇ m.
- the dye solution 1 was coated on the surface of the substrate by spin coating at a rotation rate of 1500 rpm to form a layer. This layer was dried at 70°C for 2 hours to provide a light interference layer having a film thickness of 80 nm.
- the refractive index (the real part of the complex refractive index) was 1.9
- the attenuation coefficient (the imaginary part of the complex refractive index) was 0.05 at the wavelength of 780 nm.
- the refractive index and the attenuation coefficient were 2.1 and 0.04, respectively, at 680 nm while the refractive index and the attenuation coefficient were 2.5 and 0.10, respectively, at 635 nm.
- the product of the refractive index and the film thickness (ni x di) at 780 nm, 680 nm, and 635 nm is thus 152, 168, and 200, respectively.
- a dye solution 2 obtained by dissolving 0.25 g of phthalocyanine dye represented by the formula (31) into 10 ml of 1,2-dimethylcyclohexane, was coated on the light interference layer by spin coating at a rotation speed of 1600 rpm. This solution was dried at 70°C for 2 hours to form a recording layer.
- the refractive index and the attenuation coefficient were 2.2 and 0.08, respectively, at 780 nm
- the refractive index and the attenuation coefficient were 1.2 and 0.49, respectively, at 680 nm
- the refractive index and the attenuation coefficient were 1.1 and 0.34, respectively, at 635 nm.
- an Au film was formed by sputtering on this recording layer by using a sputtering device CDI-900 (available from Balzers Co.) to form a reflective layer of 100 nm thick.
- An ultraviolet curing resin SD-17 (available from Dainippon Ink Chemicals) was coated on the reflective layer by spin coating, to which an ultraviolet ray was irradiated to form a protective layer of 6 ⁇ m in thickness.
- a laser was irradiated at a linear speed of 2.8 m/sec. with a recording power of 8 mW to record EFM signals by using a writer CCD-521 (available from Phillips Co.) with a laser head for a semiconductor laser of 780 nm.
- the recorded signal was reproduced by using a commercially available CD player (YAMAHA CDX-1050; laser wavelength 786 nm) to measure the reflectance, the error rate, and I3/Itop.
- YAMAHA CDX-1050 laser wavelength 786 nm
- the recorded signal was reproduced and estimated by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor lasers of 680 nm and 635 nm to measure the reflectance, the error rate, and the degree of modulation (I3/Itop). The results were good.
- DDU-1000 available from Pulstec Industrial Co., Ltd.
- a laser was irradiated at a linear speed of 5.6 m/sec. with a recording power of 10 mW to record EFM signals by using an optical disc estimation device DDU-1000 (available from Pulstec Industrial Co., Ltd.) with a laser head for a red semiconductor laser of 680 nm and EFM encoder (available from KENWOOD).
- the recorded signal was reproduced by using an estimation device with red semiconductor laser heads for 680 nm and 635 nm to measure the reflectance, the error rate, and I3/Itop. The results were good.
- This recorded medium was played back by a commercially available CD player (YAMAHA CDX-1050; laser wavelength 786 nm) to reproduce the signal recorded with the drive (DDU-1000) at 680 nm.
- the reflectance, the error rate, and I3/Itop were then measured. The results were good values satisfying the Orange Book Standards.
- Example 27 was repeated to produce an optical recording medium except that the order of coating was reversed, i.e., the phthalocyanine dye (formula (31)) was applied as the recording layer, and on which the azo dye (Ni metal complex of formula (18)) was coated as the light interference layer.
- the phthalocyanine dye formula (31)
- the azo dye Ni metal complex of formula (18)
- the medium obtained was subjected to recording and reproduction estimation in the same manner as in Example 27. The results were good in respect to the recording characteristics at each wavelength.
- Example 27 was repeated to produce an optical recording medium except that 0.2 g of azo dye represented by the following formula (32) was used for the light interference layer.
- the film thickness of the light interference layer was 100 nm.
- the refractive index and the attenuation coefficient were 1.8 and 0.06, respectively, at 780 nm
- the refractive index and the attenuation coefficient were 2.0 and 0.05, respectively, at 680 nm
- the refractive index and the attenuation coefficient were 2.3 and 0.09, respectively, at 635 nm.
- the product of the refractive index and the film thickness (ni x di) at 780 nm, 680 nm, and 635 nm is thus 180, 200, and 230, respectively.
- the medium obtained was subjected to recording and reproduction estimation in the same manner as in Example 27. As a result, the recording characteristics were good at each wavelength.
- Example 29 was repeated to produce an optical recording medium except that the order of application was reversed, i.e., the phthalocyanine dye (formula (31)) was applied as the recording layer, on which the azo dye (formula (32)) was coated as the light interference layer.
- the phthalocyanine dye formula (31)
- the azo dye formula (32)
- the medium obtained was subjected to recording and reproduction estimation in the same manner as in Example 27. As a result, the recording characteristics were good at each wavelength.
- Example 28 was repeated to produce a medium with the light interference layer for estimation except that the dye used was a combination of metal complexes of the azo dyes, which were represented by the formulae (18), and (20) through (23), and the phthalocyanine dyes represented by the formulae (28) through (31).
- Table 7 shows combinations of the dyes, the optical constants (refractive index (n) and attenuation coefficient (k)) of the recording and light interference layers at 780, 680, and 635 nm, the film thickness (d) of the light interference layer, and the product of the refractive index and the film thickness, i.e., ni x di.
- All media were in a high-to-low recording mode with a large degree of modulation at 780 nm, 680 nm, and 635 nm.
- the error rate and the jitter value were small to provide good reproduction.
- Example 27 was repeated to produce an optical recording medium except that the film thickness of the azo dye of the light interference layer was changed to 35 nm.
- the product of the refractive index and the film thickness (ni x di) at 780, 680, and 635 nm were 64, 74, and 88, respectively.
- the medium obtained was estimated in the same manner as in Example 27. As a result, the reproduced signal had a waveform with deformation at 680 and 635 nm. In addition, the reflectance was low.
- Example 27 was repeated to produce an optical recording medium except that the film thickness of the azo dye of the light interference layer was changed to 160 nm.
- the product of the refractive index and the film thickness (ni x di) at 780, 680, and 635 nm were 304, 336, and 400, respectively.
- the medium obtained was estimated in the same manner as in Example 27. As a result, the reproduced signal had a waveform with deformation at 786, 680 and 635 nm. In addition, the reflectance was low.
- Example 28 was repeated to produce an optical recording medium except that only the recording layer was applied.
- the medium obtained was estimated in the same manner as in Example 27. As a result, the reproduced signal had a waveform with deformation at 680 and 635 nm. In addition, the reflectance was low.
- Table 8 shows the characteristics (reflectance, error rate, and degree of modulation) of the reproduced signal obtained at wavelengths of 786, 680, and 635 nm for cases where the signals were recorded at 780 and 680 nm in Examples 27 through 37 and Comparative Examples 15 through 17.
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Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
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JP7034694 | 1994-04-08 | ||
JP70346/94 | 1994-04-08 | ||
JP7034694 | 1994-04-08 | ||
JP100035/94 | 1994-05-13 | ||
JP10003594 | 1994-05-13 | ||
JP10003594 | 1994-05-13 | ||
JP28970594 | 1994-11-24 | ||
JP28970594 | 1994-11-24 | ||
JP289705/94 | 1994-11-24 |
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EP0676751A1 true EP0676751A1 (de) | 1995-10-11 |
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ID=27300303
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP95105296A Expired - Lifetime EP0676751B1 (de) | 1994-04-08 | 1995-04-07 | Optisches Aufzeichnungsmedium |
Country Status (5)
Country | Link |
---|---|
US (1) | US5633106A (de) |
EP (1) | EP0676751B1 (de) |
KR (1) | KR950030074A (de) |
DE (1) | DE69521823D1 (de) |
TW (1) | TW320721B (de) |
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US5958650A (en) * | 1996-12-20 | 1999-09-28 | Ciba Specialty Chemicals Corporation | Complex polymethine dyes and their use |
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US6144631A (en) * | 1998-04-30 | 2000-11-07 | Mitsubishi Chemical Corporation | Information recording medium, and readout method and readout apparatus therefor |
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US6500510B1 (en) | 1999-11-04 | 2002-12-31 | Molecular Storage Technologies, Inc. | Molecular level optical information storage devices |
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JP2003276342A (ja) * | 2002-03-26 | 2003-09-30 | Tdk Corp | 光記録媒体 |
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JP2004209771A (ja) * | 2002-12-27 | 2004-07-29 | Fuji Photo Film Co Ltd | 光情報記録媒体 |
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JP4473768B2 (ja) * | 2005-04-14 | 2010-06-02 | 株式会社東芝 | 情報記憶媒体、再生方法及び記録方法 |
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TW200817477A (en) * | 2006-09-28 | 2008-04-16 | Fujifilm Corp | Optical information recording medium and azo-metal complx dye |
JP2009009684A (ja) * | 2007-06-01 | 2009-01-15 | Fujifilm Corp | 光情報記録媒体および情報記録方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0353393A2 (de) * | 1988-07-30 | 1990-02-07 | Taiyo Yuden Co., Ltd. | Optisches Informationsaufzeichnungsmedium |
JPH02128331A (ja) * | 1988-11-09 | 1990-05-16 | Hitachi Ltd | 光ディスク |
EP0418611A2 (de) * | 1989-08-30 | 1991-03-27 | Hitachi, Ltd. | Medium für optische Datenaufzeichnung, Verfahren und Apparat |
EP0455124A2 (de) * | 1990-04-25 | 1991-11-06 | Victor Company Of Japan, Limited | Optisches Aufzeichnungsmedium und Verfahren zu dessen Herstellung |
EP0463550A2 (de) * | 1990-06-22 | 1992-01-02 | MITSUI TOATSU CHEMICALS, Inc. | Optisches Aufzeichnungsmedium und Aufzeichnungsverfahren |
JPH0640162A (ja) * | 1992-01-22 | 1994-02-15 | Nippon Columbia Co Ltd | 光記録媒体 |
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NL7903915A (nl) * | 1979-05-18 | 1980-11-20 | Philips Nv | Informatieregistratieelement. |
US4460665A (en) * | 1981-12-28 | 1984-07-17 | Ricoh Co., Ltd. | Optical information recording medium |
EP0373643B1 (de) * | 1988-12-15 | 1998-01-21 | MITSUI TOATSU CHEMICALS, Inc. | Absorbiermittel im nahen Infrarot und Anzeige-/Aufzeichnungsmaterialien, die daraus hergestellt sind |
EP0376327B1 (de) * | 1988-12-29 | 1995-08-09 | Sony Corporation | Medium für optische Aufzeichnung |
JP2521178B2 (ja) * | 1990-03-17 | 1996-07-31 | 日本ビクター株式会社 | 光学的記録媒体円盤 |
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JP2657579B2 (ja) * | 1990-04-19 | 1997-09-24 | 富士写真フイルム株式会社 | 光情報記録媒体 |
US5270150A (en) * | 1990-04-25 | 1993-12-14 | Victor Company Of Japan, Ltd. | Optical recording medium and process for producing it |
JP2865955B2 (ja) * | 1992-09-09 | 1999-03-08 | 日本コロムビア株式会社 | 光記録媒体 |
-
1995
- 1995-04-04 US US08/416,365 patent/US5633106A/en not_active Expired - Fee Related
- 1995-04-07 EP EP95105296A patent/EP0676751B1/de not_active Expired - Lifetime
- 1995-04-07 DE DE69521823T patent/DE69521823D1/de not_active Expired - Lifetime
- 1995-04-08 KR KR1019950008183A patent/KR950030074A/ko active IP Right Grant
- 1995-04-13 TW TW084103692A patent/TW320721B/zh active
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EP0353393A2 (de) * | 1988-07-30 | 1990-02-07 | Taiyo Yuden Co., Ltd. | Optisches Informationsaufzeichnungsmedium |
US5090009A (en) * | 1988-07-30 | 1992-02-18 | Taiyo Yuden Co., Ltd. | Optical information recording medium |
JPH02128331A (ja) * | 1988-11-09 | 1990-05-16 | Hitachi Ltd | 光ディスク |
EP0418611A2 (de) * | 1989-08-30 | 1991-03-27 | Hitachi, Ltd. | Medium für optische Datenaufzeichnung, Verfahren und Apparat |
EP0455124A2 (de) * | 1990-04-25 | 1991-11-06 | Victor Company Of Japan, Limited | Optisches Aufzeichnungsmedium und Verfahren zu dessen Herstellung |
EP0463550A2 (de) * | 1990-06-22 | 1992-01-02 | MITSUI TOATSU CHEMICALS, Inc. | Optisches Aufzeichnungsmedium und Aufzeichnungsverfahren |
JPH0640162A (ja) * | 1992-01-22 | 1994-02-15 | Nippon Columbia Co Ltd | 光記録媒体 |
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PATENT ABSTRACTS OF JAPAN vol. 018, no. 259 (M - 1607) 18 May 1994 (1994-05-18) * |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5851621A (en) * | 1996-05-03 | 1998-12-22 | Ciba Specialty Chemicals Corporation | High-capacity storage media |
EP0840307A2 (de) * | 1996-11-01 | 1998-05-06 | Taiyoyuden Co., Ltd. | Medium für optische Datenaufzeichnung |
EP0840307A3 (de) * | 1996-11-01 | 1998-06-10 | Taiyoyuden Co., Ltd. | Medium für optische Datenaufzeichnung |
US5958650A (en) * | 1996-12-20 | 1999-09-28 | Ciba Specialty Chemicals Corporation | Complex polymethine dyes and their use |
US5962657A (en) * | 1996-12-20 | 1999-10-05 | Ciba Specialty Chemicals Corporation | Complex polymethine dyes and their use |
EP0982719A1 (de) * | 1997-05-08 | 2000-03-01 | Matsushita Electric Industrial Co., Ltd. | Optisches aufzeichnungsmedium und verfahren zur informationsaufzeichnung-/-wiedergabe dafür |
EP0982719A4 (de) * | 1997-05-08 | 2000-08-16 | Matsushita Electric Ind Co Ltd | Optisches aufzeichnungsmedium und verfahren zur informationsaufzeichnung-/-wiedergabe dafür |
US6338888B1 (en) | 1997-05-08 | 2002-01-15 | Matsushita Electric Industrial Co., Ltd. | Optical recording medium and method of information recording/reproduction using the same |
EP0913815A2 (de) * | 1997-11-01 | 1999-05-06 | Samsung Electronics Co., Ltd. | Verfahren und Vorrichtung zur Datenaufzeichnung und -wiedergabe auf und von optischen Platten |
EP0913815A3 (de) * | 1997-11-01 | 1999-06-16 | Samsung Electronics Co., Ltd. | Verfahren und Vorrichtung zur Datenaufzeichnung und -wiedergabe auf und von optischen Platten |
EP1107243A2 (de) * | 1999-12-01 | 2001-06-13 | Taiyo Yuden Co., Ltd. | Optisches Datenaufzeichnungsmedium |
EP1107243A3 (de) * | 1999-12-01 | 2003-05-28 | Taiyo Yuden Co., Ltd. | Optisches Datenaufzeichnungsmedium |
US6482494B2 (en) | 2000-05-03 | 2002-11-19 | Samsung Electronics Co., Ltd. | Hemicyanine dyes and optical recording media using the same |
EP1152038A1 (de) * | 2000-05-03 | 2001-11-07 | Samsung Electronics Co., Ltd. | Hemicyanin Farbstoffe und optische Aufzeichnungsmedium diese benutzend |
US7449279B2 (en) | 2001-10-25 | 2008-11-11 | Ricoh Company, Ltd. | Optical information recording medium |
WO2003034146A2 (en) * | 2002-11-01 | 2003-04-24 | Ciba Specialty Chemicals Holding Inc. | Solvent composition and process for manufacturing an optical recording medium using said composition and optical recording medium |
WO2003034146A3 (en) * | 2002-11-01 | 2003-10-30 | Ciba Sc Holding Ag | Solvent composition and process for manufacturing an optical recording medium using said composition and optical recording medium |
WO2005017886A2 (en) * | 2003-08-13 | 2005-02-24 | Koninklijke Philips Electronics N.V. | Recordable optical record carrier for multilevel and method for writing thereon |
WO2005017886A3 (en) * | 2003-08-13 | 2005-03-31 | Koninkl Philips Electronics Nv | Recordable optical record carrier for multilevel and method for writing thereon |
US7625621B2 (en) | 2004-07-29 | 2009-12-01 | Clariant Finance (Bvi) Limited | Amino antipyrine based azo ligands and their metal complexes for use as optical recording media |
EP1824687A1 (de) * | 2004-12-15 | 2007-08-29 | Ricoh Company, Ltd. | Optisches worm-aufzeichnungsmedium |
EP1824687A4 (de) * | 2004-12-15 | 2008-11-19 | Ricoh Kk | Optisches worm-aufzeichnungsmedium |
US8163366B2 (en) | 2004-12-15 | 2012-04-24 | Ricoh Company, Ltd. | Write-once-read-many optical recording medium |
EP1859444A1 (de) * | 2005-03-17 | 2007-11-28 | Ricoh Company, Ltd. | Optisches aufzeichnungsmedium |
EP1859444A4 (de) * | 2005-03-17 | 2008-09-03 | Ricoh Kk | Optisches aufzeichnungsmedium |
Also Published As
Publication number | Publication date |
---|---|
KR950030074A (ko) | 1995-11-24 |
DE69521823D1 (de) | 2001-08-30 |
US5633106A (en) | 1997-05-27 |
EP0676751B1 (de) | 2001-07-25 |
TW320721B (de) | 1997-11-21 |
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